(Q46188775)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

0 references

Sophie Mouillet-Richard

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

C Teil

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

M Lenne

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

S Hugon

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

O Taleb

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

J L Laplanche

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

publication date

1 October 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

Journal of the Neurological Sciences

1 November 2019

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

168

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

141-144

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

Novel proteinaceous infectious particles cause scrapie

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

14-3-3 protein, neuron-specific enolase, and S-100 protein in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Double-gradient DGGE for optimized detection of DNA point mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Deletion in prion protein gene in a Moroccan family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Deletions in the prion protein gene are not associated with CJD.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

New variant Creutzfeldt-Jakob disease: neurological features and diagnostic tests

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

The risk of developing Creutzfeldt-Jakob disease in subjects with the PRNP gene codon 200 point mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2899%2900179-3

10.1016/S0022-510X(99)00179-3

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10526198%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference